diffuse palmoplantar keratoderma KID syndrome ICD9:759.89 Editor note: Orphanet classifies as both AD and AR MEDGEN:777082 MESH:C536168 keratitis, ichthyosis, and deafness (KID) syndrome NANDO:1200621 MedDRA:10048786 Orphanet:477 OMIMPS:148210 NANDO:2200996 MONDO:0018781 Keratitis Ichthyosis Deafness Syndrome KID/HID syndrome Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. SCTID:2625009 ichthyosis hystrix Rheydt type UMLS:C3665333 Senter syndrome NORD:1326 keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome GARD:0003113 ectodermal dysplasia syndrome